~6 spots leftby Apr 2026

Neuromodulation to Treat Patients With Heart Failure With Preserved Ejection Fraction

Recruiting in Palo Alto (17 mi)
SS
Overseen byStavros Stavrakis, MD, PhD
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: University of Oklahoma
No Placebo Group
Approved in 2 Jurisdictions

Trial Summary

What is the purpose of this trial?

Heart failure with preserved ejection fraction (HFpEF) is a leading cause of mortality in the elderly. Outcomes of patients with HFpEF are poor and so far, no treatment has been shown to decrease morbidity or mortality. Recent animal and human studies suggest that a systemic proinflammatory state, produced by comorbidities, including aging, plays a central role in the development of HFpEF, supporting the notion that attenuating the proinflammatory state is an attractive therapeutic target for HFpEF. We have previously shown that low-level transcutaneous electrical stimulation of the vagus nerve (tVNS) suppresses inflammation in patients with atrial fibrillation. The overall objective of this proposal is to examine the effects of tVNS on diastolic dysfunction, exercise capacity and inflammation in patients with HFpEF. Our specific aims include: 1. To examine the effect of intermittent (1 hour daily for 3 months) tVNS on diastolic dysfunction and exercise capacity, relative to sham stimulation, in patients with HFpEF and 2. To examine the effect of intermittent (1 hour daily for 3 months) LLTS on inflammatory cytokines relative to sham stimulation, in patients with HFpEF. The proposed proof-of-concept studies will provide the basis for the design of further human studies using LLTS among populations with HFpEF. In light of the increasing number of elderly patients with HFpEF and the poor success of the currently available treatment options, an alternative and novel approach such as tVNS has the potential to impact clinical practice and improve health outcomes among a large number of patients. It is anticipated that these investigations will contribute to the broader understanding of the role of inflammation in the pathogenesis of HFpEF and how its inhibition can be used to provide therapeutic effects. Moreover, it is anticipated that a better understanding of how modulation of inflammation affects one of the hallmarks of HFpEF, diastolic dysfunction, will lead to the development of novel pharmacological and non-pharmacological approaches to treat this disease.

Research Team

SS

Stavros Stavrakis, MD, PhD

Principal Investigator

University of Oklahoma

Eligibility Criteria

Inclusion Criteria

age ≥ 65
diabetes
hypertension
See 1 more

Treatment Details

Interventions

  • Low Level Transcutaneous Vagus Nerve Stimulation (Neuromodulation)
Participant Groups
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Active treatmentExperimental Treatment1 Intervention
Patients will receive 1 hour of active transcutaneous low level vagal stimulation daily for 3 months
Group II: Sham controlPlacebo Group1 Intervention
Patients will receive 1 hour of sham transcutaneous low level vagal stimulation daily for 3 months

Find a Clinic Near You

Research Locations NearbySelect from list below to view details:
University of Oklahoma Health Sciences CenterOklahoma City, OK
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Who Is Running the Clinical Trial?

University of Oklahoma

Lead Sponsor

Trials
484
Patients Recruited
95,900+